Product Details

SNP ID
rs1002069
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48404744 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACGTACTTTCTGGGACCTCAGGGC[C/G]TCGCTGGCGGGAGGGGTAATAACAT
Phenotype
MIM: 609075 MIM: 601053
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FBXW12 PubMed Links

Gene Details

Gene
FBXW12
Gene Name
F-box and WD repeat domain containing 12
There are no transcripts associated with this gene.

Gene
PLXNB1
Gene Name
plexin B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130082.2 Intron NP_001123554.1
NM_002673.5 Intron NP_002664.2
XM_011533833.2 Intron XP_011532135.1
XM_011533834.1 Intron XP_011532136.1
XM_011533835.1 Intron XP_011532137.1
XM_011533836.1 Intron XP_011532138.1
XM_011533837.2 Intron XP_011532139.1
XM_017006630.1 Intron XP_016862119.1
XM_017006631.1 Intron XP_016862120.1

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